Everything about Indulines totally explained
Indulines are a series of
dyestuffs of blue, bluish-red or black shades, formed by the interaction of para-
amino azo compounds with primary monoamines in the presence of a small quantity of a
mineral acid. They were first discovered in
1863 by J. Dale and H. Caro, and since then have been examined by many
chemists.
They are derivatives of the eurhodines (aminophenazines, aminonaphthophenazines), and by means of their diazo derivatives can be de-amidated, yielding in this way azonium
salts; consequently they may be considered as amidated azonium salts. The first reaction giving a clue to their constitution was the isolation of the intermediate azophenin by O. Witt, which was proved by Fischer and Hepp to be dianilidoquinone dianil, a similar intermediate compound being found shortly afterwards in the
naphthalene series. Azophenin, C
30H
24N
4, is prepared by warming quinone dianil with
aniline; by melting together
quinone, aniline and aniline
hydrochloride; or by the action of aniline on para-nitrosophenol or para-nitrosodiphenylamine. The indulines are prepared as mentioned above from aminoazo compounds, or by condensing oxy- and amido-quinones with phenylated ortho-diamines. The indulines may be subdivided into the following groups: (1) benzindulines, derivatives of phenazine; (2) isorosindulines; and (3) rosindulines, both derived from naphthophenazine; and (4) naphthindulines, derived from naphthazine.
The rosindulines and naphthindulines have a strongly
basic character, and their
salts possess a marked red color and
fluorescence. Benzinduline (aposafranine), C
16H
13N
3, is a strong base, but can't be diazotized, unless it be dissolved in concentrated
mineral acids. When warmed with aniline it yields anilido-aposafranine, which may also be obtained by the direct
oxidation of ortho-aminodiphenylamine. Isorosinduline is obtained from quinone dichlorimide and phenyl-13-naphthylamine; rosinduline from benzeneazo-a-naphthylamine and aniline and naphthinduline from benzeneazo-a-naphthylamine and naphthylamine.
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